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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted January 19, 2002
Recall of Certain Iron Supplements
PRODUCT Ferrous Sulfate Tablets, 325 mg. (Dietary Supplement) under the Eckerd, H.E.B., Longs, Nature's Valley, Sav-on Osco by Albertson's and Ultima labels. The product is packed in 60 and 100 tablet blister strips in a carton, Recall # F-120-2.
CODE Lot Numbers OD01649, OF02547, OMB0627, OM02553, OM03538, OD01649, OF02547, OH02400, 1CA2142, OH02400, OMB0628, OF02546, OMB1226, OKB1115, OMB0629.
RECALLING FIRM/MANUFACTURER Recalling Firm: Leiner Health Products, Inc. Carson, CA, by letter on May 16, 2001.
Manufacturer: Leiner Health Products, Inc. Fort Mill, SC. Firm initiated recall is complete.
REASON The product is misbranded since it lists an incorrect tablet strength on the inner blister packs.
VOLUME OF PRODUCT IN COMMERCE 130,380 cartons.
DISTRIBUTION Nationwide.
Report a Problem
If you have experienced an unexpected and adverse reaction to a dietary supplement, nutritional product, or generic drug, we would like to hear about it, as we may investigate the problem. Please select from one of these options:
Dietary Supplement or Nutritional Product Problem Report
If you believe that a dietary supplement (e.g., vitamin, mineral, or herbal supplement) or other nutritional product has caused an unexpected, adverse reaction, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their Safety Reporting Portal at https://www.safetyreporting.hhs.gov.
Please complete the form below as accurately as possible. You may need to check the label on the product.
Thank you for submitting your report.
Generic Drug Problem Report
If you believe that a generic drug has not acted like the original drug, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their MedWatch program at the FDA MedWatch website.
Please complete the form below as accurately as possible. You may need to check the label on the drug.
Thank you for submitting your report.
